Montecino-Rodriguez E M, Loor F
Sandoz Pharma AG, Preclinical Research, Basel, Switzerland.
Immunology. 1991 Sep;74(1):121-6.
Reciprocal transfers of spleen and bone marrow cell suspensions have been performed between mice of the C57BL/6 (B6) genetic background, differing at the lymphoproliferation (lpr) locus. These immune system chimaeras were followed for almost one year after sublethal irradiation and cell reconstitution. In addition to the survival of the chimaeras, the major lymphoid organs (bone marrow, spleen, thymus and lymph nodes) were examined for cell numbers, percentages of membrane immunoglobulin-positive cells and responses to mitogenic stimulations with concanavalin and lipopolysaccharide. The [lpr----lpr] chimaeras were similar to untreated lpr mice. The [wild----lpr] did not develop the lpr-induced syndrome and remained similar to [wild----wild] chimaeras. Therefore, B6 wild haematopoietic stem cells could rescue sublethally irradiated B6 lpr mice from the lpr-induced autoimmune pathology. The radioresistant lpr environment alone was not sufficient to induce the lpr syndrome. It may however be required for its development since [lpr----wild] chimaeras displayed a profound aplasia of their lymphoid organs, together with a normal cellularity of their bone marrow. In contrast to chimaeras constructed with MRL mice, the [lpr----wild] B6 chimaeras did not die following the lpr haematopoietic stem cell transfer. Therefore, the lymphoid aplasia of [lpr----wild] radiation chimaeras does not result from an lpr graft-versus-host-like syndrome. More likely is that a normal, non-lpr, haematopoietic environment may not allow the differentiation of the lpr haematopoietic stem cells into the lymphoid lineages.
在具有C57BL/6(B6)遗传背景、在淋巴细胞增殖(lpr)位点存在差异的小鼠之间进行了脾脏和骨髓细胞悬液的相互转移。在亚致死剂量照射和细胞重建后,对这些免疫系统嵌合体进行了近一年的跟踪观察。除了观察嵌合体的存活情况外,还对主要淋巴器官(骨髓、脾脏、胸腺和淋巴结)进行了细胞数量、膜免疫球蛋白阳性细胞百分比以及对伴刀豆球蛋白和脂多糖的促有丝分裂刺激反应的检测。[lpr----lpr]嵌合体与未处理的lpr小鼠相似。[野生----lpr]嵌合体未出现lpr诱导的综合征,且与[野生----野生]嵌合体相似。因此,B6野生造血干细胞可以将亚致死剂量照射的B6 lpr小鼠从lpr诱导的自身免疫病理中拯救出来。仅抗辐射的lpr环境不足以诱导lpr综合征。然而,它的发展可能是必需的,因为[lpr----野生]嵌合体的淋巴器官出现了严重发育不全,而其骨髓细胞数量正常。与用MRL小鼠构建的嵌合体不同,[lpr----野生]B6嵌合体在进行lpr造血干细胞移植后并未死亡。因此,[lpr----野生]辐射嵌合体的淋巴发育不全并非由lpr移植物抗宿主样综合征导致。更有可能的是,正常的、非lpr的造血环境可能不允许lpr造血干细胞分化为淋巴谱系。